STRYKER FLEXIBLE CYSTONEPHROSCOPE
K-Number: K043022 · 2005-03-15
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Device Summary
Frequently Asked Questions
What is the STRYKER FLEXIBLE CYSTONEPHROSCOPE?
STRYKER FLEXIBLE CYSTONEPHROSCOPE is a medical device that received FDA 510(k) clearance on 2005-03-15. The listed applicant is Stryker Endoscopy. The 510(k) number is K043022.
When did STRYKER FLEXIBLE CYSTONEPHROSCOPE receive FDA 510(k) clearance?
STRYKER FLEXIBLE CYSTONEPHROSCOPE received FDA 510(k) clearance on 2005-03-15, under 510(k) number K043022.
Who is the listed applicant for STRYKER FLEXIBLE CYSTONEPHROSCOPE?
The FDA 510(k) record lists Stryker Endoscopy as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRYKER FLEXIBLE CYSTONEPHROSCOPE?
The FDA product code for STRYKER FLEXIBLE CYSTONEPHROSCOPE is FAJ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Stryker Endoscopy as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FAJ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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